| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62621949-62622255 | Common:2; Rare:92 | ||||
| chr11:62646566-62646778 | Common:1; Rare:87; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653504 | Common:1; Rare:72 | ||||
| chr11:62665133-62665444 | Common:6; Rare:148 | ||||
| chr11:62678866-62679197 | Rare:112 | ||||
| chr11:62706210-62706396 | Common:3; Rare:67; Clinvar (benign):5 | ||||
| chr11:62727445-62727675 | Rare:89 | ||||
| chr11:62771231-62771454 | Rare:61 | ||||
| chr11:62787335-62787440 | Common:2; Rare:75 | ||||
| chr11:62789217-62789382 | Common:1; Rare:60 | ||||
| chr11:62832014-62832291 | Common:1; Rare:97 | ||||
| chr11:62840374-62840585 | Common:2; Rare:34 | ||||
| chr11:62855881-62856176 | Rare:109 | ||||
| chr11:63369668-63369815 | Common:1; Rare:28 | ||||
| chr11:63671470-63671804 | Common:1; Rare:120 |